FDA Inspection
Sechrist Industries IncSechrist Industries Inc – FDA Inspection, Dec 15, 2017
Record Details
This FDA Inspection record concerns Sechrist Industries Inc, with an inspection on December 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5678e47d-6955-471a-a159-9a44197d0493
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1035020
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.75(a)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Sechrist Industries Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 12, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 26, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sechrist Industries Inc
- FDA Inspection 1181236 - 2022-09-14
- FDA Inspection 895597 - 2014-09-12
- FDA Inspection 654826 - 2010-03-26
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